ID

DB10363||

名称

Corylus americana pollen

描述

Corylus americana pollen is the pollen of the Corylus americana plant. Corylus americana pollen is mainly used in allergenic testing.

cas号

唯一标识码

ZGS382Y3AV

状态

组

approved,

指示

药效学

作用机制

毒性

代谢

吸收

半衰期

分类

消除途径

种类

Cell-mediated Immunity

Increased Histamine Release

Increased IgG Production

Non-Standardized Pollen Allergenic Extract

盐类

蛋白质结合

清除

同义词

language:english; code:; name;hazelnut pollen extract

国际品牌

配送量

产品

name:American Hazelnut Pollen
labeller:Greer Laboratories, Inc.
ndc-id:
ndc-product-code:22840-5430
dpd-id:
ema-product-code:
ema-ma-number:
started-marketing-on:1981-09-15
ended-marketing-on:
dosage-form:Solution
strength:0.05 g/1mL
route:Intradermal; Percutaneous; Subcutaneous
fda-application-number:BLA101833
generic:false
over-the-counter:false
approved:true
country:US
source:FDA NDC
name:American Hazelnut Pollen
labeller:Greer Laboratories, Inc.
ndc-id:
ndc-product-code:22840-2413
dpd-id:
ema-product-code:
ema-ma-number:
started-marketing-on:1981-09-15
ended-marketing-on:
dosage-form:Solution
strength:0.1 g/1mL
route:Intradermal; Percutaneous; Subcutaneous
fda-application-number:BLA101833
generic:false
over-the-counter:false
approved:true
country:US
source:FDA NDC
name:American Hazelnut Pollen
labeller:Greer Laboratories, Inc.
ndc-id:
ndc-product-code:22840-2414
dpd-id:
ema-product-code:
ema-ma-number:
started-marketing-on:1981-09-15
ended-marketing-on:
dosage-form:Solution
strength:40000 [PNU]/1mL
route:Intradermal; Percutaneous; Subcutaneous
fda-application-number:BLA101833
generic:false
over-the-counter:false
approved:true
country:US
source:FDA NDC
name:American Hazelnut Pollen
labeller:Greer Laboratories, Inc.
ndc-id:
ndc-product-code:22840-4446
dpd-id:
ema-product-code:
ema-ma-number:
started-marketing-on:1981-09-15
ended-marketing-on:
dosage-form:Solution
strength:0.05 g/1mL
route:Intradermal; Percutaneous; Subcutaneous
fda-application-number:BLA101833
generic:false
over-the-counter:false
approved:true
country:US
source:FDA NDC
name:American Hazelnut Pollen
labeller:Greer Laboratories, Inc.
ndc-id:
ndc-product-code:22840-2415
dpd-id:
ema-product-code:
ema-ma-number:
started-marketing-on:1981-09-15
ended-marketing-on:
dosage-form:Solution
strength:0.001 g/1mL
route:Intradermal; Percutaneous; Subcutaneous
fda-application-number:BLA101833
generic:false
over-the-counter:false
approved:true
country:US
source:FDA NDC
name:Center-AL - Corylus Americana Pollen
labeller:ALK-Abello, Inc.
ndc-id:
ndc-product-code:0268-0075
dpd-id:
ema-product-code:
ema-ma-number:
started-marketing-on:1975-01-15
ended-marketing-on:
dosage-form:Injection, suspension
strength:10000 [PNU]/1mL
route:Subcutaneous
fda-application-number:BLA103753
generic:false
over-the-counter:false
approved:true
country:US
source:FDA NDC
name:Corylus Americana Pollen
labeller:ALK-Abello, Inc.
ndc-id:
ndc-product-code:0268-1203
dpd-id:
ema-product-code:
ema-ma-number:
started-marketing-on:1965-01-01
ended-marketing-on:
dosage-form:Injection, solution
strength:0.10 g/1mL
route:Subcutaneous
fda-application-number:BLA103753
generic:false
over-the-counter:false
approved:true
country:US
source:FDA NDC
name:Corylus Americana Pollen
labeller:ALK-Abello, Inc.
ndc-id:
ndc-product-code:0268-1204
dpd-id:
ema-product-code:
ema-ma-number:
started-marketing-on:1965-01-01
ended-marketing-on:
dosage-form:Injection, solution
strength:0.05 g/1mL
route:Subcutaneous
fda-application-number:BLA103753
generic:false
over-the-counter:false
approved:true
country:US
source:FDA NDC
name:Corylus Americana Pollen
labeller:ALK-Abello, Inc.
ndc-id:
ndc-product-code:0268-1205
dpd-id:
ema-product-code:
ema-ma-number:
started-marketing-on:1965-01-01
ended-marketing-on:
dosage-form:Injection, solution
strength:20000 [PNU]/1mL
route:Subcutaneous
fda-application-number:BLA103753
generic:false
over-the-counter:false
approved:true
country:US
source:FDA NDC
name:Corylus Americana Pollen
labeller:ALK-Abello, Inc.
ndc-id:
ndc-product-code:0268-1206
dpd-id:
ema-product-code:
ema-ma-number:
started-marketing-on:1965-01-01
ended-marketing-on:
dosage-form:Injection, solution
strength:40000 [PNU]/1mL
route:Subcutaneous
fda-application-number:BLA103753
generic:false
over-the-counter:false
approved:true
country:US
source:FDA NDC
name:Corylus Americana Pollen
labeller:ALK-Abello, Inc.
ndc-id:
ndc-product-code:0268-6714
dpd-id:
ema-product-code:
ema-ma-number:
started-marketing-on:1965-01-01
ended-marketing-on:
dosage-form:Injection, solution
strength:0.05 g/1mL
route:Percutaneous
fda-application-number:BLA103753
generic:false
over-the-counter:false
approved:true
country:US
source:FDA NDC
name:Corylus Americana Pollen
labeller:ALK-Abello, Inc.
ndc-id:
ndc-product-code:0268-6715
dpd-id:
ema-product-code:
ema-ma-number:
started-marketing-on:1965-01-01
ended-marketing-on:
dosage-form:Injection, solution
strength:1000 [PNU]/1mL
route:Intradermal
fda-application-number:BLA103753
generic:false
over-the-counter:false
approved:true
country:US
source:FDA NDC
name:Hazelnut
labeller:Nelco Laboratories, Inc.
ndc-id:
ndc-product-code:36987-2668
dpd-id:
ema-product-code:
ema-ma-number:
started-marketing-on:1972-08-29
ended-marketing-on:
dosage-form:Injection, solution
strength:0.1 g/1mL
route:Intradermal; Subcutaneous
fda-application-number:BLA102192
generic:false
over-the-counter:false
approved:true
country:US
source:FDA NDC
name:Hazelnut
labeller:Nelco Laboratories, Inc.
ndc-id:
ndc-product-code:36987-2662
dpd-id:
ema-product-code:
ema-ma-number:
started-marketing-on:1972-08-29
ended-marketing-on:
dosage-form:Injection, solution
strength:10000 [PNU]/1mL
route:Intradermal; Subcutaneous
fda-application-number:BLA102192
generic:false
over-the-counter:false
approved:true
country:US
source:FDA NDC
name:Hazelnut
labeller:Nelco Laboratories, Inc.
ndc-id:
ndc-product-code:36987-2663
dpd-id:
ema-product-code:
ema-ma-number:
started-marketing-on:1972-08-29
ended-marketing-on:
dosage-form:Injection, solution
strength:20000 [PNU]/1mL
route:Intradermal; Subcutaneous
fda-application-number:BLA102192
generic:false
over-the-counter:false
approved:true
country:US
source:FDA NDC
name:Hazelnut
labeller:Nelco Laboratories, Inc.
ndc-id:
ndc-product-code:36987-2665
dpd-id:
ema-product-code:
ema-ma-number:
started-marketing-on:1972-08-29
ended-marketing-on:
dosage-form:Injection, solution
strength:40000 [PNU]/1mL
route:Intradermal; Subcutaneous
fda-application-number:BLA102192
generic:false
over-the-counter:false
approved:true
country:US
source:FDA NDC
name:Hazelnut
labeller:Nelco Laboratories, Inc.
ndc-id:
ndc-product-code:36987-2664
dpd-id:
ema-product-code:
ema-ma-number:
started-marketing-on:1972-08-29
ended-marketing-on:
dosage-form:Injection, solution
strength:20000 [PNU]/1mL
route:Intradermal; Subcutaneous
fda-application-number:BLA102192
generic:false
over-the-counter:false
approved:true
country:US
source:FDA NDC
name:Hazelnut
labeller:Nelco Laboratories, Inc.
ndc-id:
ndc-product-code:36987-2667
dpd-id:
ema-product-code:
ema-ma-number:
started-marketing-on:1972-08-29
ended-marketing-on:
dosage-form:Injection, solution
strength:0.05 g/1mL
route:Intradermal; Subcutaneous
fda-application-number:BLA102192
generic:false
over-the-counter:false
approved:true
country:US
source:FDA NDC
name:Hazelnut
labeller:Nelco Laboratories, Inc.
ndc-id:
ndc-product-code:36987-2666
dpd-id:
ema-product-code:
ema-ma-number:
started-marketing-on:1972-08-29
ended-marketing-on:
dosage-form:Injection, solution
strength:0.05 g/1mL
route:Intradermal; Subcutaneous
fda-application-number:BLA102192
generic:false
over-the-counter:false
approved:true
country:US
source:FDA NDC
name:Hazelnut
labeller:Nelco Laboratories, Inc.
ndc-id:
ndc-product-code:36987-2661
dpd-id:
ema-product-code:
ema-ma-number:
started-marketing-on:1972-08-29
ended-marketing-on:
dosage-form:Injection, solution
strength:10000 [PNU]/1mL
route:Intradermal; Subcutaneous
fda-application-number:BLA102192
generic:false
over-the-counter:false
approved:true
country:US
source:FDA NDC
name:Hazelnut Pollen
labeller:Antigen Laboratories, Inc.
ndc-id:
ndc-product-code:49288-0261
dpd-id:
ema-product-code:
ema-ma-number:
started-marketing-on:1974-03-23
ended-marketing-on:
dosage-form:Injection, solution
strength:0.05 g/1mL
route:Intradermal; Subcutaneous
fda-application-number:BLA102223
generic:false
over-the-counter:false
approved:true
country:US
source:FDA NDC
name:Hazelnut Pollen
labeller:Allermed Laboratories, Inc.
ndc-id:
ndc-product-code:49643-340
dpd-id:
ema-product-code:
ema-ma-number:
started-marketing-on:1974-03-12
ended-marketing-on:
dosage-form:Injection
strength:0.05 g/1mL
route:Cutaneous; Intradermal; Subcutaneous
fda-application-number:BLA102211
generic:false
over-the-counter:false
approved:true
country:US
source:FDA NDC

混合物

name:Hazelnut Pollen
ingredients:Corylus americana pollen
name:Hazelnut
ingredients:Corylus americana pollen
name:Hazelnut
ingredients:Corylus americana pollen
name:Hazelnut
ingredients:Corylus americana pollen
name:Hazelnut
ingredients:Corylus americana pollen
name:Hazelnut
ingredients:Corylus americana pollen
name:Hazelnut
ingredients:Corylus americana pollen
name:Hazelnut
ingredients:Corylus americana pollen
name:Hazelnut
ingredients:Corylus americana pollen
name:Hazelnut Pollen
ingredients:Corylus americana pollen
name:American Hazelnut Pollen
ingredients:Corylus americana pollen
name:American Hazelnut Pollen
ingredients:Corylus americana pollen
name:American Hazelnut Pollen
ingredients:Corylus americana pollen
name:American Hazelnut Pollen
ingredients:Corylus americana pollen
name:American Hazelnut Pollen
ingredients:Corylus americana pollen
name:Center-AL - Corylus Americana Pollen
ingredients:Corylus americana pollen
name:Corylus Americana Pollen
ingredients:Corylus americana pollen
name:Corylus Americana Pollen
ingredients:Corylus americana pollen
name:Corylus Americana Pollen
ingredients:Corylus americana pollen
name:Corylus Americana Pollen
ingredients:Corylus americana pollen
name:Corylus Americana Pollen
ingredients:Corylus americana pollen
name:Corylus Americana Pollen
ingredients:Corylus americana pollen

包装者

生产者

价格

受影响的生物体

剂量

form:Solution
route:Intradermal; Percutaneous; Subcutaneous
strength:0.001 g/1mL
form:Solution
route:Intradermal; Percutaneous; Subcutaneous
strength:0.05 g/1mL
form:Solution
route:Intradermal; Percutaneous; Subcutaneous
strength:0.1 g/1mL
form:Solution
route:Intradermal; Percutaneous; Subcutaneous
strength:40000 [PNU]/1mL
form:Injection, suspension
route:Subcutaneous
strength:10000 [PNU]/1mL
form:Injection, solution
route:Intradermal
strength:1000 [PNU]/1mL
form:Injection, solution
route:Percutaneous
strength:0.05 g/1mL
form:Injection, solution
route:Subcutaneous
strength:0.05 g/1mL
form:Injection, solution
route:Subcutaneous
strength:0.10 g/1mL
form:Injection, solution
route:Subcutaneous
strength:20000 [PNU]/1mL
form:Injection, solution
route:Subcutaneous
strength:40000 [PNU]/1mL
form:Injection, solution
route:Intradermal; Subcutaneous
strength:0.1 g/1mL
form:Injection, solution
route:Intradermal; Subcutaneous
strength:10000 [PNU]/1mL
form:Injection, solution
route:Intradermal; Subcutaneous
strength:20000 [PNU]/1mL
form:Injection, solution
route:Intradermal; Subcutaneous
strength:40000 [PNU]/1mL
form:Injection
route:Cutaneous; Intradermal; Subcutaneous
strength:0.05 g/1mL
form:Injection, solution
route:Intradermal; Subcutaneous
strength:0.05 g/1mL

atc代码

fda标签

化学品安全技术说明书

专利

食物相互作用

药物相互作用

序列

实验性质

外部标识符

resource：PubChem Substance
identifier：347910540
resource：RxCUI
identifier：852281

外部链接

路径

目标

酶

载体

运输工具

药物反应

效应

不良反应